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Infrared study of carbon monoxide hydrogenation over rhodium/ceria and rhodium/silica catalysts

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100378a061· OSTI ID:6331694
; ;  [1]; ; ;  [2]
  1. Universite de Caen (France)
  2. Laboratoire de Chimie Organique Appliquee, Strasbourg (France)
Carbon monoxide hydrogenation over ceria-promoted Rh or Rh/SiO{sub 2} catalysts was investigated by means of Fourier transform infrared spectroscopy. In the chemisorption of CO at room temperature, a new absorption band was observed near 1,725 or 1,696 cm{sup {minus}1} on a reduced 5% Rh-5% CeO{sub 2}/SiO{sub 2} or 5% Rh/CeO{sub 2} catalyst, respectively. This new absorption band was attributed to a C- and O-bonded species, located at the metal/support interface. The appearance of this species was related to the shift to lower temperatures of the peak ascribed to CO dissociation in the temperature-programmed desorption spectra after CO adsorption. A flow high-pressure IR cell allowed to study the surface species in situ during CO + H{sub 2} reaction and to follow the reactivity of these species toward pure H{sub 2}. The results suggest that the drop in methane formation may be related to a lower reactivity of surface carbon in the presence of the promoter.
OSTI ID:
6331694
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 94:15; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English